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Evaluation of platelet surface glycoproteins in patients with Glanzmann thrombasthenia: Association with bleeding symptoms

BACKGROUND & OBJECTIVES: Glanzmann thrombasthenia (GT) is a rare, inherited autosomal recessive disorder characterized by qualitative or quantitative deficiency of integrin αIIbβ3 [glycoprotein IIb (GPIIb)/IIIa, CD41/CD61] diagnosed by absent or reduced platelet aggregation to physiological agon...

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Detalles Bibliográficos
Autores principales:	Mutreja, Deepti, Sharma, Rahul Kumar, Purohit, Abhishek, Aggarwal, Mukul, Saxena, Renu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2017
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5644297/ https://www.ncbi.nlm.nih.gov/pubmed/28948953 http://dx.doi.org/10.4103/ijmr.IJMR_718_14

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